Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,644 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,644 in last 12 months

Showing 39013920 of 49,990 recalls

FoodNovember 1, 2024· Lithuanian Bakery, Inc.

Recalled Item: Chocolate Raspberry: Three sizes Recalled by Lithuanian Bakery, Inc. Due to...

The Issue: Products contain undeclared allergens (milk, soy, peanut, and wheat) and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cinnamon Rolls 16.5oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cheese Danish 16.5 oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· JR Watkins

Recalled Item: Cooling Menthol Extra Strength Pain Relief Patch Recalled by JR Watkins Due...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 2L4C Instrument US Recalled by Becton, Dickinson and Company, BD...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L12C Instrument RUO Recalled by Becton, Dickinson and Company, BD...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L10C Instrument US-IVD Recalled by Becton, Dickinson and Company,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L8C Instrument US-IVD Recalled by Becton, Dickinson and Company,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: Device Description: FACSLyric 2L6C Instrument US Recalled by Becton,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Medtronic Neurosurgery

Recalled Item: Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA...

The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2024· Medtronic Neurosurgery

Recalled Item: Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER...

The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health SMS Elastic Cuff Thumbhook Level 3 Isolation Gown Recalled...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Convertor Isolation Gown Recalled by Cardinal Health 200, LLC Due to...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Securitas Healthcare LLC

Recalled Item: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...

The Issue: Certain software versions will not notify end users of calls initiated by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing